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Open nowPosted 12 hours agoWe saw it 40 min after it went up

Strategist / Senior Strategist - Regulatory Affairs

ClinChoice52 open roles

Where
Bengaluru, Karnataka, India
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Your applicationOpen nowStrategist / Senior Strategist - Regulatory AffairsClinChoice · Bengaluru, Karnataka, India

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on ClinChoice's own form.

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The clock on this job

Early applications get read.

9.8% of postings close within 7 days. Measured by our own scanner across the market. ClinChoice postings stay open a median of 27 days.

Share of postings closed within
  1. 1.9%1 day
  2. 3.9%3 days
  3. 9.8%7 days
  4. 15.5%14 days
  5. 33.8%30 days
This job: posted 12 hours ago

ClinChoice median: 27 days open

The posting

Responsibilities:

  • Supports UK, Ireland, Malta, Sweden, Finland, Norway, and Denmark products across the product portfolio.
  • Supports the team with regulatory strategies (local and regional) that are in line with the business plan
  • Supports the team with regulatory activities for National and/or European procedures (Decentralized, Mutual Recognition) as appropriate. For example, but not limited to: Prepares and compiles regulatory submissions, response to questions, renewals, post submission/approval activities (including relevant updates to external websites such as emc, medicines.ie and In-Demand) Supports ad hoc projects (e.g., compliance reviews, audit preparation etc.) Signs off on packaging material, leaflets, and SmPCs (as appropriate)
  • Supports the compilation of the Northern Cluster team metrics for the EMEA biannual metrics report
  • Supports all regulatory activities in Malta
  • Ensures regulatory compliance within the department to include: The maintenance of global, regional, and local databases Adherence to processes, SOPs, work instructions, and job aids Updates to relevant local and global databases to track current product information
  • Supports team with Calls for Information (CFI) and assist in any Pharmacovigilance- related activities within the Northern Cluster, which may include: Receiving and monitoring responses to CFIs through liaison with UK and EAME colleagues Ensuring responses are submitted in a timely manner and that they are in line with standard procedures and metrics established by the VP Regulatory Affairs in European Regulatory Provide support and responses to ad hoc requests received from UK PV group or Global Reg Med Mailbox
  • Supports the team with regulatory activities for National and/or European procedures (Decentralized, Mutual Recognition) as appropriate.
  • Ensures regulatory compliance within the department

Experience/Qualifications:

  • Bachelor's/Master's degree in Life Science/Pharma
  • Minimum of 5 ~ 8 years of relevant work experience working within a Regulatory Affairs Department (e.g., pharmaceutical, cosmetic, food supplements, etc.), with direct accountability for deliverables or a combination of direct Regulatory Affairs experience of CMC, Quality, or Regulatory Operations.
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